Episode 7 · MAPASGEN · PRO

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Test: Your Hedonistic Profile — What Your Tastes Say About Your DNA

Episode 7 · MAPASGEN · PRO Material

Level: practical · Topic: nutrigenomics, taste genetics, personalised nutrition

This test is not a diagnosis and not a substitute for DNA analysis. It is a tool for self-observation: your answers point to likely variants of several key taste-related genes. After each question — a breakdown of what lies behind your choice at the molecular level.

Part 1. The Test — 8 Questions

Question 1. How do you feel about coriander (cilantro)?

A) I love it — fresh, bright aroma

B) Neutral — I don't notice anything particular

C) I can't stand it — tastes like soap or chemicals

Breakdown: Answer C indicates the presence of a functional allele of OR6A2. This receptor is highly sensitive to aldehydes (decenal, trans-2-decenal) that form the core of coriander's aroma. Carriers of the sensitive variant literally perceive a different smell — not 'herbal' but 'soapy' or 'chemical.' This is one of the best-documented genetic taste phenomena: the association was confirmed in a 2012 GWAS study of more than 25,000 participants (Eriksson et al., Flavour journal).

Question 2. How many cups of coffee do you drink daily — and when is your last one?

A) 1–2, the last one before noon — otherwise I can't sleep

B) 2–4, the last one by 3 pm

C) 4 or more; I can drink in the evening with no effect on sleep

Breakdown: Answer A is a marker of a slow caffeine metaboliser (CYP1A2 *1F). Caffeine clears slowly; the effect is long-lasting. Answer C points to a fast metaboliser (*1A): caffeine is broken down within 2–3 hours, requiring more for a sustained effect. In raw DNA data, look for SNP rs762551: allele A = fast metabolism, allele C = slow.

Question 3. How do you feel about broccoli, Brussels sprouts, grapefruit?

A) Unbearably bitter — I can't eat them

B) Slightly bitter but manageable

C) I notice no bitterness at all

Breakdown: Answer A suggests a supertaster — most likely a PAV/PAV genotype of TAS2R38 (both alleles 'sensitive'). Answer B indicates medium sensitivity, a PAV/AVI heterozygote. Answer C is a non-taster, AVI/AVI. SNPs to check: rs713598, rs1726866, rs10246939. The combination of these three SNPs determines the functional status of the receptor.

Question 4. Do you flush after 1–2 drinks?

A) Yes, strongly — and sometimes feel nauseous

B) Slightly, but it passes quickly

C) Never

Breakdown: Answer A suggests a high probability of the ALDH2*2 variant (especially with East Asian ancestry) or an active ADH1B*2 variant, in which ethanol is rapidly converted to acetaldehyde but the latter accumulates. Medical context: ALDH2*2 carriers who drink regularly have an elevated risk of oesophageal cancer. SNPs to check: rs671 (ALDH2), rs1229984 (ADH1B).

Question 5. How do you feel about spicy food?

A) I love it — the hotter the better

B) In moderation

C) I can't tolerate it at all — even mild spice is uncomfortable

Breakdown: This is linked to the TRPV1 gene — the vanilloid receptor that responds to capsaicin (the active compound in chilli). Answer A is often associated with lower baseline TRPV1 sensitivity and/or neural adaptation from regular exposure. More in the Premium material.

Question 6. Do you taste bitterness in red wine (especially tannins)?

A) Yes — red wine tastes very bitter and astringent to me

B) Slightly — I prefer softer wines

C) No — I barely notice any bitterness

Breakdown: TAS2R38 again — it also responds to tannins. Supertasters generally prefer white or rosé wines with low tannin content, or avoid wine altogether in favour of lighter drinks. Non-tasters comfortably drink full-bodied, highly tannic reds.

Question 7. Is sweetness a reward or a matter of indifference?

A) A reward — I love sweet things and find it hard to stop

B) Neutral — I can take it or leave it

C) Indifferent — I prefer savoury or sour

Breakdown: The sweetness receptor is encoded by TAS1R2 and TAS1R3. Variants of TAS1R2 (notably SNP rs35874116) are associated with varying sensitivity to sucrose and sweet food consumption. Answer A may indicate heightened receptor sensitivity, or variants in dopamine-system genes (DRD2) that amplify the reward signal from sweet foods.

Question 8. How well do you tolerate fatty food?

A) Well — I enjoy it and digest it easily

B) Fine in moderate amounts

C) Poorly — I feel heavy or uncomfortable after fatty meals

Breakdown: CD36 encodes a fatty acid receptor on the tongue's surface. Its variants affect how intensely you perceive the taste of fat. The APOE gene (particularly the ε4 allele) influences fat metabolism — carriers process saturated fats less efficiently and have an elevated cardiovascular risk on a high-fat diet.

Part 2. How to Find These Markers in Your DNA Test

All of the SNPs listed are accessible in the raw data of most consumer DNA tests (23andMe, AncestryDNA, MyHeritage). The process:

  1. Download your raw data.
  2. Open the file in a text editor or upload it to Promethease / Genetic Genie.
  3. Search by rs number: rs762551 (caffeine), rs713598 + rs1726866 + rs10246939 (bitterness), rs671 (alcohol/ALDH2), rs1229984 (alcohol/ADH1B).
  4. Compare the alleles you find with the breakdowns in the test above.

An important limitation: Each of these genes is one factor among dozens that influence taste perception. Epigenetics, the microbiome, childhood experience, culture, and habit contribute no less. DNA is a predisposition, not a sentence.

Part 3. Practical Applications: Personalised Nutrition

Knowing your taste genetic profile offers several practical advantages:

— Premium Material —

Premium contains a full science-writing longreid on spiciness: the evolutionary puzzle of chilli, the neurochemistry of capsaicin, the TRPV1 gene, and why spice lovers live longer (spoiler: the correlation exists; causation is debated).

MAPASGEN — the podcast about genetics that is already reshaping your life.


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